Haryana Dhillon

Haryana Dhillon

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2016 in Clinical Psychology Review
Verified
Journal Article
Closed access
ZSZac Seidler
Zac Seidler
ADAlexei J. Dawes
Alexei J. Dawes
Simon M. RiceSimon M. Rice
Simon M. Rice
JOJohn Oliffe
John Oliffe
HDHaryana Dhillon
Haryana Dhillon

22 October 2015 in New England Journal of Medicine
Verified
Journal Article
Closed access
PDF file
ACAndrew C. Chen
Andrew C. Chen
AMAndrew J. Martin
Andrew J. Martin
BCBonita Choy
Bonita Choy
PFPablo Fernandez-Peñas
Pablo Fernandez-Peñas
RDRobyn A. Dalziell
Robyn A. Dalziell
DDDiona L. Damian
Diona L. Damian
Nonmelanoma skin cancers, such as basal-cell carcinoma and squamous-cell carcinoma, are common cancers that are caused principally by ultraviolet (UV) radiation. Nicotinamide (vitamin B3) has been shown to have protective effects against damage caused by UV radiation and to reduce the rate of new premalignant actinic keratoses.

1 April 2015 in The Lancet
Verified
Journal Article
Closed access
JHJolyn Hersch
Jolyn Hersch
ABAlexandra Barratt
Alexandra Barratt
JJJesse Jansen
Jesse Jansen
LILes Irwig
Les Irwig
KMKevin McGeechan
Kevin McGeechan
KMKirsten McCaffery
Kirsten McCaffery

1 December 2015 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
JVJanette Vardy
Janette Vardy
HDHaryana Dhillon
Haryana Dhillon
GPGregory R. Pond
Gregory R. Pond
SRSean B. Rourke
Sean B. Rourke
TBTsegaye Bekele
Tsegaye Bekele
ITIan F. Tannock
Ian F. Tannock
Purpose: Cognitive dysfunction is reported in people with cancer. Therefore, we evaluated longitudinal changes in cognitive function and underlying mechanisms in people with colorectal cancer (CRC) and healthy controls (HCs). Patients and Methods: Participants completed cognitive assessments and questionnaires reporting cognitive symptoms, fatigue, quality of life, and anxiety/depression at baseline (before chemotherapy, if given) and 6, 12, and 24 months. Blood tests included cytokines, clotting factors, apolipoprotein E genotype, and sex hormones. Primary end point was overall cognitive function measured by the Global Deficit Score at 12 months. Results: We recruited 289 patients with localized CRC (173 received chemotherapy; median age, 59 years; 63% male), 73 patients with limited metastatic/recurrent CRC, and 72 HCs. Cognitive impairment was more frequent in patients with localized CRC than HCs at baseline (43% v 15%, respectively; P < .001) and 12 months (46% v 13%, respectively; P < .001), with no significant effect of chemotherapy. Attention/working memory, verbal learning/memory, and complex processing speed were most affected. Cognitive impairment was similar in patients with localized and metastatic CRC. Cytokine levels were elevated in patients with CRC compared with HCs. There was no association between overall cognitive function and fatigue, quality of life, anxiety/depression, or any blood test. Cognitive symptoms at 12 months were reported in 25% of patients with localized CRC versus 17% of HCs (P = .19). More participants who received chemotherapy had cognitive symptoms at 6 months (32%) versus those who did not (16%; P = .007), with no significant difference at 12 months (29% v 21%, respectively; P = .19). Objective cognitive function was only weakly associated with cognitive symptoms. Conclusion: Patients with CRC had substantially more cognitive impairment at every assessment than HCs, with no significant added effect of chemotherapy. Mechanisms of cognitive impairment remain unknown.

10 January 2017 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
VBVictoria J. Bray
Victoria J. Bray
HDHaryana Dhillon
Haryana Dhillon
MBMelanie L Bell
Melanie L Bell
MKMichael Kabourakis
Michael Kabourakis
MFMallorie H. Fiero
Mallorie H. Fiero
JVJanette Vardy
Janette Vardy
Purpose: Cognitive impairment is reported frequently by cancer survivors. There are no proven treatments. We evaluated a cognitive rehabilitation program (Insight) and compared it with standard care in cancer survivors self-reporting cognitive symptoms. Patients and Methods: We recruited adult cancer survivors with a primary malignancy (excluding central nervous system malignancies) who had completed three or more cycles of adjuvant chemotherapy in the previous 6 to 60 months and reported persistent cognitive symptoms. All participants received a 30-minute telephone consultation and were then randomly assigned to the 15-week, home-based intervention or to standard care. Primary outcome was self-reported cognitive function (Functional Assessment of Cancer Therapy Cognitive Function [FACT-COG] perceived cognitive impairment [PCI] subscale): difference between groups after intervention (T2) and 6 months later (T3). Results: A total of 242 participants were randomly assigned: median age, 53 years; 95% female. The primary outcome of difference in FACT-COG PCI was significant, with less PCI in the intervention group at T2 ( P < .001). This difference was sustained at T3 ( P < .001). At T2, there was a significant difference in all FACT-COG subscales, favoring the intervention. Neuropsychological results were not significantly different between the groups at T2 or T3. There were significantly lower levels of anxiety/depression and fatigue in the intervention group at T2. There were significant improvements in stress in the intervention group at both time points. There was no significant difference in quality of life between the groups at T2, but the intervention group had better quality of life at T3. Conclusion: The intervention, Insight, led to improvements in cognitive symptoms compared with standard care. To our knowledge, this is the first large randomized controlled trial showing an improvement in self-reported cognitive function in cancer survivors, indicating that this intervention is a feasible treatment.

23 January 2013 in BMJ
Verified
Journal Article
Open access
PDF file
JHJolyn Hersch
Jolyn Hersch
JJJesse Jansen
Jesse Jansen
ABAlexandra Barratt
Alexandra Barratt
LILes Irwig
Les Irwig
NHNehmat Houssami
Nehmat Houssami
KMKirsten McCaffery
Kirsten McCaffery
Objective To elicit women’s responses to information about the nature and extent of overdiagnosis in mammography screening (detecting disease that would not present clinically during the woman’s lifetime) and explore how awareness of overdiagnosis might influence attitudes and intentions about screening. Design Qualitative study using focus groups that included a presentation explaining overdiagnosis, incorporating different published estimates of its rate (1–10%, 30%, 50%) and information on the mortality benefit of screening, with guided group discussions Setting Sydney, Australia Participants Fifty women aged 40–79 years with no personal history of breast cancer and with varying levels of education and participation in screening. Results Prior awareness of breast cancer overdiagnosis was minimal. Women generally reacted with surprise, but most came to understand the issue. Responses to overdiagnosis and the different estimates of its magnitude were diverse. The highest estimate (50%) made some women perceive a need for more careful personal decision making about screening. In contrast, the lower and intermediate estimates (1–10% and 30%) had limited impact on attitudes and intentions, with many women remaining committed to screening. For some women, the information raised concerns, not about whether to screen but whether to treat a screen detected cancer or consider alternative approaches (such as watchful waiting). Information preferences varied: many women considered it important to take overdiagnosis into account and make informed choices about whether to have screening, but many wanted to be encouraged to be screened. Conclusions Women from a range of socioeconomic backgrounds could comprehend the issue of overdiagnosis in mammography screening, and they generally valued information about it. Effects on screening intentions may depend heavily on the rate of overdiagnosis. Overdiagnosis will be new and counterintuitive for many people and may influence screening and treatment decisions in unintended ways, underscoring the need for careful communication.